Gorla R, Airò P, Malagoli A, Carella G, Prati E, Brugnoni D, Franceschini F, Cattaneo R
Servizio di Immunologia Clinica, Spedali Civili di Brescia, Italy.
Clin Rheumatol. 1994 Mar;13(1):83-7. doi: 10.1007/BF02229871.
Systemic Sclerosis (SSc; scleroderma) is associated with several immunological abnormalities, including altered proportion between lymphocyte subsets. Peripheral blood lymphocyte subsets from 25 patients with SSc were studied by two-colour flow cytometry using monoclonal antibodies against CD45RA and CD29 markers, which allow a dissection of CD4+ and CD8+ populations into 'naive' and 'memory' subsets. A decrease of the percentage of CD8+ (p < 0.05) and of CD8+CD29+ (p < 0.001) cells was observed compared to that in 20 age and sex-matched controls. These abnormalities were not significantly associated with the extension of cutaneous disease or other clinical features of SSc nor with treatment, pattern of autoantibodies or HLA phenotype.
系统性硬化症(SSc;硬皮病)与多种免疫异常有关,包括淋巴细胞亚群比例改变。使用抗CD45RA和CD29标志物的单克隆抗体,通过双色流式细胞术研究了25例系统性硬化症患者的外周血淋巴细胞亚群,这使得可以将CD4+和CD8+群体分为“初始”和“记忆”亚群。与20名年龄和性别匹配的对照相比,观察到CD8+细胞(p < 0.05)和CD8+CD29+细胞(p < 0.001)的百分比降低。这些异常与皮肤疾病的范围或系统性硬化症的其他临床特征均无显著关联,也与治疗、自身抗体模式或HLA表型无关。